Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (40): 6520-6525.doi: 10.3969/j.issn.2095-4344.2015.40.023

Previous Articles     Next Articles

An experimental model of chronic renal allograft rejection in SD-Wistar rats

Yu Peng-cheng1, Liu Yong-guang2, Guo Ying2, Li Min2, Xiao Zong-yu3, Hu Kong-he4, Huang Jin-jun5,    Xin Jun6, Wu Zhi-qiang2, Zhao Ming2   

  1. 1Department of Nephrology, 6Department of Urology, Quanzhou First Hospital, Fujian Medical University, Quanzhou 362000, Fujian Province, China; 2Organ Transplant Center, 3Department of Neurosurgery, 4Department of Orthopedics, 5Department of Plastic Surgery, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, Guangdong Province, China
  • Online:2015-09-30 Published:2015-09-30
  • Contact: Zhao Ming, M.D., Chief physician, Professor, Doctoral supervisor, Organ Transplant Center, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, Guangdong Province, China
  • About author:Yu Peng-cheng, M.D., Associate chief physician, Department of Nephrology, Quanzhou First Hospital, Fujian Medical University, Quanzhou 362000, Fujian Province, China
  • Supported by:

    a grant from Science and Technology Planning Project of Quanzhou City of China, No. 2009Z39

Abstract:

BACKGROUND: Fisher-Lewis rat kidney transplant models are the international common chronic renal allograft rejection models, but their application is greatly limited because of difficulty in model preparation and high costs.

OBJECTIVE: To explore a new method of establishing SD-Wistar rat models of chronic renal allograft rejection.

METHODS: Fifty-six pairs of SD-Wistar rats were subjected to left kidney orthotopic transplantation. The right kidneys of the recipients were intact and used as internal controls. 23 rat recipients were randomly divided into model group (n=15) and control group (n=8). The rats in the model group were injected with cyclosporine microemulsion for 10 days (2 mg/kg/day,i.p.) after kidney transplantation. The rats in the control group were not treated with immunosuppressive therapy.

RESULTS AND CONCLUSION: The irreversible acute rejection occurred in all the transplanted kidneys of rats in the control group within 4 weeks, leading to the necrosis of transplanted kidney. Moderate inflammatory cell infiltration appeared in the transplanted kidneys of rats in the model group at 4, 8 and 12 weeks after transplantation. Typical histopathological changes of chronic rejection were observed within 12 weeks after transplantation. The Banff total scores were increased with time after transplantation. All these histopathological changes were not observed in the intact right kidneys of rat recipients in both groups. The valley value of cyclosporine concentration in the transplanted rats in the model group was (153.2±17.1) μg/L at 4 days after transplantation. These results demonstrate that after a short course treatment of cyclosporine microemulsion (2 mg/kg/day for 10 days, i.p.) in SD-Wistar rat recipients, moderate inflammatory cell infiltration was followed by development of chronic rejection within 12 weeks, and such animal models can be used for studying chronic renal allograft rejection.

中国组织工程研究杂志出版内容重点:肾移植肝移植移植;心脏移植;组织移植;皮肤移植;皮瓣移植;血管移植;器官移植组织工程

Key words: Transplantation, Kidney Transplantation, Graft Rejection, Cyclosporine

CLC Number: